Dan M. Roden
Vanderbilt University
Public scientific profile · Unclaimed
Built from public scholarly sources. Expertise is inferred by ScienceWe from publications and has not been confirmed by the scientist.
Top expertise
Cardiac electrophysiology and arrhythmias
Strong evidence · 6 supporting papers · latest 2026
Genetic Associations and Epidemiology
Strong evidence · 2 supporting papers · latest 2026
Cardiomyopathy and Myosin Studies
Strong evidence · 3 supporting papers · latest 2026
Chronic Lymphocytic Leukemia Research
Solid evidence · 1 supporting paper · latest 2026
Genomics and Rare Diseases
Solid evidence · 5 supporting papers · latest 2026
Cardiovascular Effects of Exercise
Solid evidence · 2 supporting papers · latest 2026
Lung Cancer Treatments and Mutations
Solid evidence · 1 supporting paper · latest 2026
Congenital heart defects research
Solid evidence · 2 supporting papers · latest 2026
Publications (14)
Systematic common and rare variant association testing in 392,030 whole genomes in All of Us
2026DOIPMID 42180372
Ventricular conduction is a marker for arrhythmic risk in SCN5A- E1784K overlap sodium channel disease
2026DOIPMID 42114100
Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome
2026DOIPMID 42465902
CASTing a shadow over the design of gene therapy trials
2026DOIPMID 42580470
Damaging RBM20 E-rich domain variants are not rescued by gene replacement
2026DOIPMID 42523282
Ibrutinib therapy results in atrial fibrillation through modulation of the Src-Erk1/2 pathway
2026DOI
Scaled Multidimensional Assays of Variant Effect Identify Sequence-Function Relationships in Hypertrophic Cardiomyopathy
2026DOIPMID 40501845
Association of Common Ancestry-Enriched Variants With Cardiomyopathy and Arrhythmias
2026DOIPMID 42200287
Entrectinib results in ventricular tachycardia and Brugada phenocopy through inhibition of sodium current
2026DOIPMID 42015242
Prevalence and Clinical Impact of Pathogenic Variants in Cardiomyopathy Genes Among Individuals with Cardiac Conduction Disorders
2026DOIPMID 42369476
AP-534523-003 GENETIC SCREENING OF FAMILY MEMBERS IN AN ATRIAL FIBRILLATION PRECISION MEDICINE CLINIC
2026DOI
PO-02-299 SOMATIC MOSAICISM AS A CAUSE OF FALSE NEGATIVE MOLECULAR AUTOPSY IN INFANT SUDDEN DEATH
2026DOI
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants
2026DOI
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants
2026DOI
Organizations in sourced records
Affiliation evidence only — not confirmed current employment.
- Vanderbilt University
Source: OpenAlex · retrieved 2026-09-29